Device, hemostasis, vascular
PMA 核准號：P960043 · 2026-09-24
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器材摘要
Device, hemostasis, vascular is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Vascular, Inc.. It received FDA 510(k) clearance on 2026-09-24. The device is classified under product code MGB. It was reviewed by the CV advisory panel.
常見問題
What is the Device, hemostasis, vascular?
Device, hemostasis, vascular is a medical device that received FDA 510(k) clearance on 2026-09-24. The listed applicant is Abbott Vascular, Inc..
When did Device, hemostasis, vascular receive FDA 510(k) clearance?
The clearance date for Device, hemostasis, vascular can be found in the official FDA records.
Who is the listed applicant for Device, hemostasis, vascular?
The FDA 510(k) record lists Abbott Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Device, hemostasis, vascular?
The FDA product code for Device, hemostasis, vascular is MGB.
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官方來源
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